Literature DB >> 16877628

Impact of privacy legislation on the number and characteristics of people who are recruited for research: a randomised controlled trial.

L Trevena1, L Irwig, A Barratt.   

Abstract

BACKGROUND: Privacy laws have recently created restrictions on how researchers can approach study participants.
METHOD: In a randomised trial of 152 patients, 50-74 years old, in a family practice, 60 were randomly selected to opt-out and 92 to opt-in methods. Patients were sent an introductory letter by their doctor in two phases, opt-out before and opt-in after introduction of the new Privacy Legislation in December 2001. Opt-out patients were contacted by researchers. Opt-in patients were contacted if patients responded by email, free telephone number or a reply-paid card.
RESULTS: Opt-in recruited fewer patients (47%; 43/92) after invitation compared with opt-out (67%; 40/60); (-20%; [-4% to -36%]). No proportional difference in recruitment was found between opt-in and opt-out groups varied by age, sex or socioeconomic status. The opt-in group had significantly more people in active decision-making roles (+30%; [10% to 50%]; p = 0.003). Non-significant trends were observed towards opt-in being less likely to include people with lower education (-11.8%; [-30% to 6.4%]; p = 0.13) and people who were not screened (-19.1%; [-40.1% to 1.9%]; p = 0.08). Opt-in was more likely to recruit people with a family history of colorectal cancer (+12.7%; [-2.8%, 28.2%]; p = 0.12).
CONCLUSIONS: The number of participants required to be approached was markedly increased in opt-in recruitment. Existing participants (eg, screening attendees) with a vested interest such as increased risk, and those preferring an active role in health decision making and with less education were likely to be recruited in opt-in. Research costs and generalisability are affected by implementing privacy legislation.

Entities:  

Mesh:

Year:  2006        PMID: 16877628      PMCID: PMC2563378          DOI: 10.1136/jme.2004.011320

Source DB:  PubMed          Journal:  J Med Ethics        ISSN: 0306-6800            Impact factor:   2.903


  13 in total

1.  Medical privacy and medical research--judging the new federal regulations.

Authors:  George J Annas
Journal:  N Engl J Med       Date:  2002-01-17       Impact factor: 91.245

2.  The effect of the new federal medical-privacy rule on research.

Authors:  Jennifer Kulynych; David Korn
Journal:  N Engl J Med       Date:  2002-01-17       Impact factor: 91.245

3.  Effects of changes to Data Protection Act.

Authors:  A J Silman; G J Macfarlane
Journal:  Lancet       Date:  2001-05-05       Impact factor: 79.321

Review 4.  The new HIPAA (Health Insurance Portability and Accountability Act of 1996) Medical Privacy Rule: help or hindrance for clinical research?

Authors:  Jennifer Kulynych; David Korn
Journal:  Circulation       Date:  2003-08-26       Impact factor: 29.690

5.  Low health literacy called a major problem.

Authors:  Brian Vastag
Journal:  JAMA       Date:  2004-05-12       Impact factor: 56.272

6.  Data protection, informed consent, and research.

Authors:  Julian Peto; Olivia Fletcher; Clare Gilham
Journal:  BMJ       Date:  2004-05-01

7.  Representativeness of samples from general practice lists in epidemiological studies: case-control study.

Authors:  A G Smith; N T Fear; G R Law; E Roman
Journal:  BMJ       Date:  2004-02-27

8.  Privacy: bad for your health?

Authors:  Kerry-Ann F O'Grady; Terence M Nolan
Journal:  Med J Aust       Date:  2004-03-15       Impact factor: 7.738

9.  Selection bias from requiring patients to give consent to examine data for health services research.

Authors:  S H Woolf; S F Rothemich; R E Johnson; D W Marsland
Journal:  Arch Fam Med       Date:  2000 Nov-Dec

10.  Decision making during serious illness: what role do patients really want to play?

Authors:  L F Degner; J A Sloan
Journal:  J Clin Epidemiol       Date:  1992-09       Impact factor: 6.437

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  20 in total

Review 1.  Recruiting participants for injury studies in emergency departments.

Authors:  Denise Kendrick; Ronan Lyons; Nicola Christie; Elizabeth Towner; Jonathan Benger; Lindsay Groom; Frank Coffey; Phillip Miller; Rachel Murphy
Journal:  Inj Prev       Date:  2007-04       Impact factor: 2.399

2.  The impact of HIPAA authorization on willingness to participate in clinical research.

Authors:  Anne L Dunlop; Tracie Graham; Zanie Leroy; Karen Glanz; Boadie Dunlop
Journal:  Ann Epidemiol       Date:  2007-08-06       Impact factor: 3.797

3.  An exploration of the cultural context of kinship and genetics amongst Arabic-Australians: implications for practice.

Authors:  Mona Saleh; Kristine Barlow-Stewart; Bettina Meiser; Judy Kirk; Kathy Tucker
Journal:  J Genet Couns       Date:  2011-05-10       Impact factor: 2.537

4.  Heightened attention to medical privacy: challenges for unbiased sample recruitment and a possible solution.

Authors:  Ann Butler Nattinger; Liliana E Pezzin; Rodney A Sparapani; Joan M Neuner; Toni K King; Purushottam W Laud
Journal:  Am J Epidemiol       Date:  2010-07-21       Impact factor: 4.897

5.  A Psycho-Educational Intervention for People with a Family History of Depression: Pilot Results.

Authors:  Bettina Meiser; Michelle Peate; Charlene Levitan; Philip B Mitchell; Lyndal Trevena; Kristine Barlow-Stewart; Timothy Dobbins; Helen Christensen; Kerry A Sherman; Kate Dunlop; Peter R Schofield
Journal:  J Genet Couns       Date:  2016-09-29       Impact factor: 2.537

6.  A randomised controlled trial to compare opt-in and opt-out parental consent for childhood vaccine safety surveillance using data linkage: study protocol.

Authors:  Jesia G Berry; Philip Ryan; Annette J Braunack-Mayer; Katherine M Duszynski; Vicki Xafis; Michael S Gold
Journal:  Trials       Date:  2011-01-04       Impact factor: 2.279

Review 7.  Strategies to improve recruitment to randomised trials.

Authors:  Shaun Treweek; Marie Pitkethly; Jonathan Cook; Cynthia Fraser; Elizabeth Mitchell; Frank Sullivan; Catherine Jackson; Tyna K Taskila; Heidi Gardner
Journal:  Cochrane Database Syst Rev       Date:  2018-02-22

8.  Methods to improve recruitment to randomised controlled trials: Cochrane systematic review and meta-analysis.

Authors:  Shaun Treweek; Pauline Lockhart; Marie Pitkethly; Jonathan A Cook; Monica Kjeldstrøm; Marit Johansen; Taina K Taskila; Frank M Sullivan; Sue Wilson; Catherine Jackson; Ritu Jones; Elizabeth D Mitchell
Journal:  BMJ Open       Date:  2013-02-07       Impact factor: 2.692

9.  Strategies to improve retention in randomised trials.

Authors:  Katie Gillies; Anna Kearney; Ciara Keenan; Shaun Treweek; Jemma Hudson; Valerie C Brueton; Thomas Conway; Andrew Hunter; Louise Murphy; Peter J Carr; Greta Rait; Paul Manson; Magaly Aceves-Martins
Journal:  Cochrane Database Syst Rev       Date:  2021-03-06

10.  When "no" might not quite mean "no"; the importance of informed and meaningful non-consent: results from a survey of individuals refusing participation in a health-related research project.

Authors:  Brian Williams; Linda Irvine; Alison R McGinnis; Marion E T McMurdo; Iain K Crombie
Journal:  BMC Health Serv Res       Date:  2007-04-26       Impact factor: 2.655

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